Canonical Allele Identifier: CA2259228139
Gene: ERBB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39725106G= , CM000679.2:g.39725106G= GRCh38
NC_000017.10:g.37881359G= , CM000679.1:g.37881359G= GRCh37
NC_000017.9:g.35134885G= NCBI36
NG_007503.1:g.41967G= , LRG_724:g.41967G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2551G= MANE Select ENSP00000269571.4:p.Val851=
ENST00000269571.9:c.2551G= ENSP00000269571.4:p.Val851=
ENST00000406381.6:c.2461G= ENSP00000385185.2:p.Val821=
ENST00000445658.6:c.1723G= ENSP00000404047.2:p.Val575=
ENST00000541774.5:c.2506G= ENSP00000446466.1:p.Val836=
ENST00000578373.5:c.*2341G= ENSP00000463427.1:n.*2341G=
ENST00000580074.1:c.657G=
ENST00000583038.5:n.3685G=
ENST00000584450.5:c.2551G= ENSP00000463714.1:p.Val851=
ENST00000584601.5:c.2461G= ENSP00000462438.1:p.Val821=
NM_001005862.2:c.2461G= , LRG_724t1:c.2461G= NP_001005862.1:p.Val821=
NM_001289936.1:c.2506G= , LRG_724t4:c.2506G= NP_001276865.1:p.Val836=
NM_001289937.1:c.2551G= NP_001276866.1:p.Val851=
NM_004448.3:c.2551G= , LRG_724t2:c.2551G= NP_004439.2:p.Val851=
NR_110535.1:n.2875G=
XM_024450641.1:c.2689G= XP_024306409.1:p.Val897=
XM_024450642.1:c.2644G= XP_024306410.1:p.Val882=
XM_024450643.1:c.2599G= XP_024306411.1:p.Val867=
NM_001005862.3:c.2461G= NP_001005862.1:p.Val821=
NM_001289936.2:c.2506G= NP_001276865.1:p.Val836=
NM_001289937.2:c.2551G= NP_001276866.1:p.Val851=
NM_001382782.1:c.2461G= NP_001369711.1:p.Val821=
NM_001382783.1:c.2461G= NP_001369712.1:p.Val821=
NM_001382784.1:c.2668G= NP_001369713.1:p.Val890=
NM_001382785.1:c.2653G= NP_001369714.1:p.Val885=
NM_001382786.1:c.2632G= NP_001369715.1:p.Val878=
NM_001382787.1:c.2626G= NP_001369716.1:p.Val876=
NM_001382788.1:c.2581G= NP_001369717.1:p.Val861=
NM_001382789.1:c.2572G= NP_001369718.1:p.Val858=
NM_001382790.1:c.2548G= NP_001369719.1:p.Val850=
NM_001382791.1:c.2542G= NP_001369720.1:p.Val848=
NM_001382792.1:c.2515G= NP_001369721.1:p.Val839=
NM_001382793.1:c.2509G= NP_001369722.1:p.Val837=
NM_001382794.1:c.2509G= NP_001369723.1:p.Val837=
NM_001382795.1:c.2503G= NP_001369724.1:p.Val835=
NM_001382796.1:c.2551G= NP_001369725.1:p.Val851=
NM_001382797.1:c.2452G= NP_001369726.1:p.Val818=
NM_001382798.1:c.2493+195G= NP_001369727.1:n.2493+195G=
NM_001382799.1:c.2371G= NP_001369728.1:p.Val791=
NM_001382800.1:c.2365G= NP_001369729.1:p.Val789=
NM_001382801.1:c.2445+195G= NP_001369730.1:n.2445+195G=
NM_001382802.1:c.2293G= NP_001369731.1:p.Val765=
NM_001382803.1:c.2509G= NP_001369732.1:p.Val837=
NM_001382804.1:c.1723G= NP_001369733.1:p.Val575=
NM_001382805.1:c.2208+1446G= NP_001369734.1:n.2208+1446G=
NM_001382806.1:c.1513G= NP_001369735.1:p.Val505=
NM_004448.4:c.2551G= MANE Select NP_004439.2:p.Val851=
NR_110535.2:n.2789G=